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US6264984B1 - Effervescent histamine H2 antagonist composition - Google Patents

Effervescent histamine H2 antagonist composition Download PDF

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US6264984B1
US6264984B1 US09455233 US45523399A US6264984B1 US 6264984 B1 US6264984 B1 US 6264984B1 US 09455233 US09455233 US 09455233 US 45523399 A US45523399 A US 45523399A US 6264984 B1 US6264984 B1 US 6264984B1
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acid
acidulant
composition
containing
group
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US09455233
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Mamoun M. Hussein
John Migton
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Novartis AG
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Bristol-Myers Squibb Co
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425Thiazoles
    • A61K31/4261,3-Thiazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/34Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • A61K31/341Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide not condensed with another ring, e.g. ranitidine, furosemide, bufetolol, muscarine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0002Galenical forms characterised by the drug release technique; Application systems commanded by energy
    • A61K9/0007Effervescent

Abstract

A histamine H2 antagonist incompatible with acidic materials is incorporated in an effervescent composition and is stable therein provided the acidulant employed in the effervescent couple is a non-hydroxy group containing acidulant and such acidulant is employed as substantially the entire amount of the acidulant present in the formulation. Preferably the composition is devoid of hydroxy group containing acidulant. Adipic acid, succinic acid, fumaric acid and succinic anhyride may be employed as the acidulant. Adipic acid is preferred.

Description

FIELD OF THE INVENTION

This invention relates to effervescent compositions containing histamine H2 antagonists incompatible with acidulants and more particularly, it relates to effervescent histamine H2 antagonists containing compositions containing certain acidulants found to be compatible with such antagonists.

BACKGROUND OF THE INVENTION

Effervescent compositions usually comprise excipients, active ingredients, and a source of carbon dioxide typically referred to as an effeverscent couple. Effervescent couples are usually composed of an alkaline bicarbonate or carbonate and an acid. In the presence of water, the alkaline bicarbonate or carbonate and the acid generate carbon dioxide. Thus, effeverscent compositions are extremely sensitive to moisture. This necessitates special steps to protect the raw materials and the finished formulation from exposure to moisture, throughout the manufacturing process and thereafter. Anhydrous citric acid is the most commonly employed acidulant in the manufacture of effeverscent compositions. Anhydrous citric acid is however, extremely hygroscopic. So also are the most commonly employed sources of carbon dioxide, i.e, alkali bicarbonates and carbonates.

The aforementioned problems are compounded when an effervescent composition is to contain, as the active, a histamine H2 antagonist. Histamine H2 antagonists are incompatible with acids, particularly the acids employed in effervescent compositions. Published EP Patent specification No. 233853 discloses that use of citric acid in effervescent compositions containing a histamine H2 antagonist evidences incompatibility of the H2 antagonist with the acids contained in the effervescent composition. In an effort to resolve this, citric acid was replaced by a mixture of mono- and di- alkaline citrates.

U.S. Pat. No. 4,824,664 teaches that histamine H2 antagonists are not stable with the acids contained in effervescent products. They endeavor to overcome this instability by granulating the effervescent mixture and generating during such granulation a mixture of mono- and di- alkali citrate in a specified ratio.

U.S. Pat. No. 5,102,665 teaches preparation of a stable effervescent ranitidine using mono-alkali citrate as the sole acidulant. The effervescent system disclosed therein is granulated in alcohol prior to manufacturing the composition.

SUMMARY OF THE INVENTION

In light of the above teaching of the prior art, one skilled in the art would, in view of the known incompatibility of histamine H2 antagonists, and in particular, ranitidine, with acids employed in effervescent products would refrain from making such a combination. Surprisingly and unexpectedly, the present inventors have discovered that certain acids (i.e., non-hydroxy group containing acidulants) can be incorporated in effervescent compositions containing histamine H2 antagonists and that the resultant compositions are stable. In other words, surprisingly and unexpectedly, the histamine H2 antagonists are stable in effervescent compositions of the present invention.

DETAILED DESCRIPTION OF THE INVENTION

The acidulants that can be utilized in preparing the effervescent histamine H2 antagonist compositions of the present invention are non-hydroxy group containing acidulants. For example, adipic acid, succinic acid, fumaric acid or a derivative thereof that hydrolyzes to form a non-hydroxy group containing acidulants, for example, succinic anhydride.

Although small amounts of a hydroxy containing acidulant may be incorporated in the effervescent composition of the present invention, the composition of the present invention most desirably employs as substantially all of the acidulant, a non-hydroxy group containing acidulant. Most preferably the composition of the present invention is devoid of hydroxy group containing acidulant. In some instances a very small amount of hydroxy group containing acidulant can be tolerated in the composition.

As noted earlier, the present inventors discovered that citric acid, a hydroxy group containing acidulant typically employed in effervescent compositions is incompatible with histamine H2 antagonists when they are incorporated in effervescent compositions. Moreover, malic acid and other hydroxy group containing acidulants present even more of a problem than citric acid. Tartaric acid also presents a compatibility problem, but less than citric acid.

Surprisingly and unexpectedly, the present inventors discovered that when the hydroxy group containing acidulant (such as citric acid and tartaric acid) employed in a histamine H2 antagonist containing effervescent formulation, as part of the effervescent couple, is replaced by a non-hydroxy group containing acidulant (such as adipic acid or succinic acid), in an amount equivalent to the hydroxy group containing acidulant, the resultant effervescent product has acceptable taste, stability and effervescence. Thus, the present invention enables the preparation of histamine H2 antagonist containing effervescent products, by simple dry mixing of ingredients without the need for alkaline metal mono- or di- citrates, (whether added as such, or generated in the effervescent system by wet granulation) and without the need for an effervescent couple containing citric acid.

The compositions of the present invention contain, as an active, a histamine H2 antagonist. The histamine H2 antagonist is preferably selected from the group consisting of ranitidine, cimetidine, famotidine and nizatidine, and pharmaceutically acceptable salts thereof. Ranitidine and cimetidine are more preferred. Ranitidine and its pharmaceutically acceptable salts are most preferred.

The amount of ranitidine, in the form of its salt, may be from 40 to 300 mg, preferably in the range of 50 to 150 mg and most preferably from 50 to 75 mg per dosage unit.

The histamine H2 antagonist is generally present in the composition in an amount such that a dose of the composition will contain such amount of the histamine H2 antagonist as has been approved by the applicable governmental health authority for prescriptive (“Rx”) or over-the-counter (“O.T.C.”) use. In the United States such amounts are as follows:

OTC Dose Rx Dose
Ranitidine 75 mg 150-300 mg
Cimetidine 200 mg  300-800 mg
Famotidine 10 mg 20-40 mg
Nizatidine 75 mg 150-300 mg

The effervescent couple employed in the compositions of the present invention is comprised of an alkaline component and an acidulant. The alkaline component and the acidulant react in the presence of water to produce carbon dioxide (i.e., effervescence). As noted earlier, the acidulant should be substantially comprised of one or more non-hydroxy group containing acidulant. Adipic acid, succinic acid, fumaric acid and succinic anhydride are preferred. Succinic anhydride will hydrolyze to form succinic acid.

As the alkaline component of the effervescent couple, sodium bicarbonate, sodium carbonate, potassium carbonate, potassium bicarbonate, calcium carbonate, magnesium carbonate, sodium glycine carbonate and mixtures thereof may be employed.

The amounts of acid and alkaline bicarbonate or carbonate may each separately constitute 25 to 60% (w/w), more preferably 30 to 50% (w/w), of the effervescent composition. The equivalent or stoichiometric ratio of acid to alkaline carbonate or bicarbonate may be within the range of 1:2 to 2: 1.

The composition of the present invention can include sweetening agents such as sucrose, aspartame, cyclamic acid salts, acesulfame-K, saccharin acid or its salts, and mixtures thereof. Filler and flow promoting materials can also be employed, for example, silicon dioxide.

To illusethe benefits of the instant invention an effervescent formulation according to Example 1 which follows, was prepared. The amount of ranitidine hydrochloride used in all of the examples is equivalent to 75 mg. ranitidine, i.e., the OTC dose in the United States.) The acidulant was varied, as is shown in Examples 2 through 6 which follow.

EXAMPLE 1

The following prototype powder effervescent histamine H2 antagonist composition was prepared. Although any histamine H2 antagonists could be employed with like results, ranitidine hydrochloride was employed in all examples.

The composition was prepared by blending all ingredients in a twin shell blender until a uniform composition was obtained. The composition had the formula:

INGREDIENT %(WT/WT) AMOUNT(g./sachet)
Sodium bicarbonate 45.25 2.29
Sodium carbonate (anhydrous) 4.54 0.23
Adipic Acid 43.86 2.22
Sucrose 2.17 0.11
Silicon Dioxide 0.10 0.005
Ranitidine hydrochloride 1.66 0.084
Aspartame 0.40 0.02
Glycine (aminoacetic acid) 1.98 0.10
Sodium Saccharin 0.04 0.002
TOTAL 100.00 5.061

EXAMPLE 2

The composition as described in Example 1 was prepared except that instead of 2.22 g/sachet adipic acid, 1.95 g/sachet of citric acid were employed.

EXAMPLE 3

The composition of Example 1 was prepared except that instead of 2.22 g/sachet adipic acid, 2.04 g/sachet of malic acid were employed.

EXAMPLE 4

The composition of Example 1 was prepared except that instead of 2.22 g./sachet adipic acid, 2.29 g/sachet of tartaric acid were employed.

EXAMPLE 5

The composition of Example 1 was prepared except that instead of 2.22 g./sachet adipic acid, 1.80 g/sachet succinic acid were employed.

It should be noted that the amount of acidulant employed in each of Examples 2 through 5 was an amount equivalent to the amount of adipic acid employed in Example 1. In other words, in all of the examples, stoichiometrically equivalent amounts of acidulants were employed.

EXAMPLE 6

Equivalent amounts of each of the compositions of Examples 1, 2, 3, 4 and 5 were stored at ambient temperature and exposed to the atmosphere. The physical appearance of each composition was determined after 12 days of such storage. The results are shown in Table 1 below.

It should be noted that Examples 1 and 5 are examples in accordance with the instant invention, whereas Examples 2, 3 and 4 are examples wherein the acidulant employed is a hydroxy group containing acidulant and as such in not in accordance with the instant invention.

TABLE 1
PHYSICAL APPEARANCE
EXAMPLE NUMBER ACIDULANT AFTER 12 DAYS EXPOSURE
2 Citric acid Heavily caked & not free
flowing
No discoloration
3 Malic acid Heavily caked & not free
flowing
Strong discoloration
4 Tartaric acid Some caking, but free flowing
No color change
1 Adipic acid No caking and free flowing
no color change
5 Succinic acid no caking and free flowing
no color change

It should be noted that the compositions of Examples 1 and 5, respectively containing adipic acid and succinic acid, were allowed to remain exposed to the atmosphere for 16 more days. In other words, for a total of four weeks. The compositions of each of Examples 1 and 5 continued to exhibit no caking, were free flowing and showed no color change.

EXAMPLE 7

Equivalent amounts of the compositions according to Examples 2, 3, 1 and 5 were packaged in vials. The vials were closed and stored at 40° C. and thereafter observed. The results are shown in Table 2 below.

TABLE 2
PHYSICAL APPEARANCE
AFTER THE INDICATED
EXAMPLE NUMBER ACIDULANT PERIOD OF STORAGE
2 Citric acid Heavily caked & slightly
discolored after 3 days
3 Malic acid Heavily caked & slightly
discolored after 3 days
5 Succinic acid Free flowing with very slight
color change after
4 weeks, and still free flowing
after 10 weeks
1 Adipic acid free flowing with no color
change after 4 weeks, and still
free flowing with no color
change after 13 weeks

EXAMPLE 8

As noted earlier, the prior art teaches that ranitidine is incompatible with acids. To assess the degree of such incompatibility, the present inventors prepared binary mixtures containing ranitidine plus an acidulant in a 1:1 ratio. These mixtures were then subjected to varied temperature and relative humidity storage conditions, as set forth in Table 3 below.

TABLE 3
% Ranitidine Remaining After Storage at:
1:1 mixture of: 30° C./60% RH 35° C./75% RH 40° C./75% RH
Ranitidine: 85.7 70.3 28.4
Citric acid*
Ranitidine: 63.9 18.9 2.3
Malic acid**
Ranitidine: 97.7 67.9 37.6
Tartaric acid*
Ranitidine: 100.1 84.5 63.9
Adipic acid**
*Determination made after 8 weeks storage.
**Determination made after 6 weeks storage.

The data of Table 3 was generated utilizing a very high ratio of ranitidine to acid. Additionally, a variation in humidity and temperature was employed. This was done to accelerate any degradation that might occur.

It is abundantly clear from the data of Table 3 that even under the extreme conditions in which ranitidine was evaluated, ranitidine is vastly more stable with adipic acid (a non-hydroxy group containing acidulant) than with citric, malic or tartaric acids (hydroxy group containing acidulants). This is entirely unexpected and surprising.

EXAMPLE 9

To demonstrate that the acidulant employed in the effervescent composition of the present invention should preferably be comprised substantially entirely of non-hydroxy group containing acidulant and more specifically should preferably be devoid of hydroxy group containing acidulants, the following composition was prepared:

INGREDIENT Amount (g/sachet) % (Wt/Wt)
Sodium Bicarbonate 2.29 43.36
Anhydrous Sodium carbonate 0.23 4.36
Adipic Acid 2.22 42.04
Tartaric Acid 0.22 4.17
Sucrose 0.11 2.08
Silicon Dioxide 0.005 0.09
Ranitidine Hydrochloride 0.084 1.59
Aspartame 0.02 0.38
Glycine 0.10 1.89
Sodium saccharin 0.002 0.04
TOTAL 5.281 100.00

The composition of the present example was prepared by admixing the powders as a dry blend, in a twin shell blender, until the mixture was uniform.

Using the same procedure, another composition was made identical to the above composition, however, the tartaric acid was omitted from the composition. Both compositions were stored at 40° C. After six weeks at that temperature the composition containing ranitidine hydrochloride, adipic acid and tartaric acid showed some discoloration. The same composition without the tartaric acid exhibited no discoloration after six week at 40° C. and more importantly, exhibited no discoloration after 13 weeks storage at 40° C. Thus, it is obvious from these results that the acidulant employed in the composition of the present invention should preferably be comprised substantially entirely of non-hydroxy group containing acidulant and most preferably should be devoid of hydroxy group containing acidulant.

Although the instant invention has been described with reference to powders and sachets, it is not limited to that dosage form. Tablets can also be produced. Example 10 which follows illustrates the preparation of tablets in accordance with the present invention.

EXAMPLE 10

The composition is as follows:

INGREDIENTS % (Wt/Wt) Grams/per tablet
Ranitidine hydrochloride 1.61 0.084
Silicon dioxide 0.1 0.005
Sodium carbonate (anhydrous) 4.41 0.23
Sodium bicarbonate 43.95 2.29
Adipic acid 42.6 2.22
Aspartame 0.38 0.02
Sodium saccharin 0.04 0.002
Glycine 1.92 0.10
Sucrose 2.11 0.11
Sodium benzoate 2.88 0.15
TOTALS 100.00 5.211

The above formulation was scaled up for 50 tablets.

Sodium benzoate was included in the formula as a soluble lubricant. One skilled in the art of tablet formation would appreciate that other lubricants could also be utilized.

The ranitidine hydrochloride was screened through a 40 mesh screen. The silicon dioxide was passed through a 20 mesh screen. The remaining ingredients were passed through a 30 mesh screen. The ingredients were dry blended and the resultant mixture was compressed on a F3 Single Punch Press. The tablets so produced were satisfactory in all respects.

It should be appreciated that the examples set forth above are merely illustrative of the present invention and are not intended to be limiting in any respect. One skilled in the art can, using ordinary skill in the art, modify the formulations illustrated above without departing from the spirit and scope of the invention.

Claims (15)

What is claimed is:
1. A powder composition comprising an effective amount of a histamine H2 antagonist, an unreacted acidulant, and an unreacted alkaline material which will react with the acidulant in the presence of water to form carbon dioxide, the acidulant being a non-hydroxy group containing acidulant that is solid at ambient conditions.
2. The composition according to claim 1, wherein the composition is free of hydroxy group containing acidulant.
3. The composition according to claim 1, wherein the non-hydroxy group containing acidulant is selected from the group consisting of adipic acid, succinic acid, fumaric acid, succinic anhydride and mixtures thereof.
4. The composition according to claim 3, wherein the non-hydroxy group containing acidulant is adipic acid.
5. The composition according to claim 3, wherein the non-hydroxy group containing acidulant is succinic acid.
6. The composition according to claim 1, wherein the Histamine H2 antagonist is selected from the group consisting of ranitidine, cimetidine, nizatidine, famotidine and pharmaceutically acceptable salts thereof.
7. The composition according to claim 1, wherein the Histamine H2 receptor antagonist is ranitidine or a pharmaceutically acceptable salt thereof.
8. A tablet comprising an effective amount of a histamine H2 antagonist, an unreacted acidulant, an unreacted alkaline material which will react with the acidulant on contact with water to form carbon dioxide, and a lubricant, said acidulant being a non-hydroxy group containing acidulant that is solid at ambient conditions.
9. The tablet according to claim 8, wherein the Histamine H2 receptor antagonist is selected from the group consisting of ranitidine, cimetidine, nizatidine, famotidine and pharmaceutically acceptable salts thereof.
10. The composition according to claim 9, wherein the Histamine H2 receptor antagonist is ranitidine or a pharmaceutically acceptable salt thereof.
11. The tablet according to claim 8, wherein the non-hydroxy group containing acidulant is selected from the group consisting of adipic acid, succinic acid, fumaric acid, succinic anhydride and mixtures thereof.
12. The composition according to claim 11, wherein the non-hydroxy group containing acidulant is adipic acid.
13. The composition according to claim 11, wherein the non-hydroxy group containing acidulant is succinic acid.
14. The composition according to claim 1, wherein the composition is free of hydroxy group containing acidulant.
15. The tablet according to claim 8 wherein the tablet is free of hydroxy group containing acidulant.
US09455233 1999-12-06 1999-12-06 Effervescent histamine H2 antagonist composition Active US6264984B1 (en)

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US09455233 US6264984B1 (en) 1999-12-06 1999-12-06 Effervescent histamine H2 antagonist composition

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US09455233 US6264984B1 (en) 1999-12-06 1999-12-06 Effervescent histamine H2 antagonist composition
DE2000624132 DE60024132T2 (en) 1999-12-06 2000-11-16 A histamine-2 antagonists h containing effervescent composition
EP20000980395 EP1237543B1 (en) 1999-12-06 2000-11-16 Effervescent histamine h2 antagonist composition
DK00980395T DK1237543T3 (en) 1999-12-06 2000-11-16 A composition comprising effervescent histamine H2 antagonist
CN 00816772 CN1211077C (en) 1999-12-06 2000-11-16 Histamine H2 antagonist effervescent composition
JP2001541483A JP2003515553A (en) 1999-12-06 2000-11-16 Effervescent histamine h2 antagonist composition
CA 2394902 CA2394902C (en) 1999-12-06 2000-11-16 Effervescent histamine h2 antagonist composition
DE2000624132 DE60024132D1 (en) 1999-12-06 2000-11-16 A histamine-2 antagonists h containing effervescent composition
ES00980395T ES2252078T3 (en) 1999-12-06 2000-11-16 Effervescent composition h2 antagonist of histamine.
PCT/US2000/031360 WO2001039750A1 (en) 1999-12-06 2000-11-16 Effervescent histamine h2 antagonist composition

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CA (1) CA2394902C (en)
DE (2) DE60024132T2 (en)
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070154542A1 (en) * 2005-12-30 2007-07-05 Cogentus Pharmaceuticals, Inc. Oral pharmaceutical formulations containing non-steroidal anti-inflammatory drugs and acid inhibitors
US20150290174A1 (en) * 2014-04-11 2015-10-15 Resuscitate MOE LLC Pharmaceutical formulations and method of using the same for alleviating symptoms of hangover, stomach flu or migraine

Citations (10)

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Publication number Priority date Publication date Assignee Title
US4824664A (en) 1986-01-22 1989-04-25 Laboratoires Smith Kline & French Effervescent couples, histamine H2 -antagonist effervescent compositions containing them and their preparation
US5102665A (en) 1988-06-24 1992-04-07 Glaxo Group Limited Pharmaceutical compositions
WO1995010274A1 (en) 1993-10-14 1995-04-20 F.H. Faulding & Co. Limited Aqueous pharmaceutical composition
US5424075A (en) 1991-03-27 1995-06-13 Miles Inc. Delivery system for enhanced onset and increased potency
EP0670160A1 (en) 1994-03-01 1995-09-06 Gerhard Dr. Gergely Granular product or tablet containing an effervescent system and an active pharmaceutical substance, as well as a method for its preparation
US5503846A (en) * 1993-03-17 1996-04-02 Cima Labs, Inc. Base coated acid particles and effervescent formulation incorporating same
EP0761212A2 (en) 1995-09-08 1997-03-12 Takeda Chemical Industries, Ltd. Effervescent composition and its production
US5759575A (en) 1993-09-09 1998-06-02 Gerhard Gergely Effervescent granules and process for their preparation
US5762951A (en) 1990-09-04 1998-06-09 Bayer Aktiengesellschaft Effervescent composition and tablet made there from
US5792473A (en) 1994-03-01 1998-08-11 Gerhard Gergely Granular product or tablet containing an effervescent system and an active pharmaceutical substance, as well as a method for its preparation

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Publication number Priority date Publication date Assignee Title
US5728401A (en) * 1997-04-16 1998-03-17 Ranbaxy Laboratories, Ltd. Effervescent ranitidine formulations

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4824664A (en) 1986-01-22 1989-04-25 Laboratoires Smith Kline & French Effervescent couples, histamine H2 -antagonist effervescent compositions containing them and their preparation
EP0233853B1 (en) 1986-01-22 1990-09-12 Laboratoires SMITH KLINE & FRENCH Effervescent couples, effervescent compositions of h2-antagonists of histamine and their preparation
US5102665A (en) 1988-06-24 1992-04-07 Glaxo Group Limited Pharmaceutical compositions
US5762951A (en) 1990-09-04 1998-06-09 Bayer Aktiengesellschaft Effervescent composition and tablet made there from
US5424075A (en) 1991-03-27 1995-06-13 Miles Inc. Delivery system for enhanced onset and increased potency
US5503846A (en) * 1993-03-17 1996-04-02 Cima Labs, Inc. Base coated acid particles and effervescent formulation incorporating same
US5759575A (en) 1993-09-09 1998-06-02 Gerhard Gergely Effervescent granules and process for their preparation
WO1995010274A1 (en) 1993-10-14 1995-04-20 F.H. Faulding & Co. Limited Aqueous pharmaceutical composition
EP0670160A1 (en) 1994-03-01 1995-09-06 Gerhard Dr. Gergely Granular product or tablet containing an effervescent system and an active pharmaceutical substance, as well as a method for its preparation
US5792473A (en) 1994-03-01 1998-08-11 Gerhard Gergely Granular product or tablet containing an effervescent system and an active pharmaceutical substance, as well as a method for its preparation
EP0761212A2 (en) 1995-09-08 1997-03-12 Takeda Chemical Industries, Ltd. Effervescent composition and its production

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070154542A1 (en) * 2005-12-30 2007-07-05 Cogentus Pharmaceuticals, Inc. Oral pharmaceutical formulations containing non-steroidal anti-inflammatory drugs and acid inhibitors
US20150290174A1 (en) * 2014-04-11 2015-10-15 Resuscitate MOE LLC Pharmaceutical formulations and method of using the same for alleviating symptoms of hangover, stomach flu or migraine

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DE60024132D1 (en) 2005-12-22 grant
EP1237543B1 (en) 2005-11-16 grant
CA2394902A1 (en) 2001-06-07 application
WO2001039750A1 (en) 2001-06-07 application
CA2394902C (en) 2006-08-08 grant
EP1237543A4 (en) 2004-06-30 application
CN1211077C (en) 2005-07-20 grant
ES2252078T3 (en) 2006-05-16 grant
DK1237543T3 (en) 2006-01-16 grant
EP1237543A1 (en) 2002-09-11 application
JP2003515553A (en) 2003-05-07 application
CN1407885A (en) 2003-04-02 application
DE60024132T2 (en) 2006-08-03 grant

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